Canonical Allele Identifier: CA2653411138

Gene: CSTF1

Linked Data

• gnomAD v4: 20-56392955-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.56392960dup , CM000682.2:g.56392960dup	GRCh38
NC_000020.10:g.54968016dup , CM000682.1:g.54968016dup	GRCh37
NC_000020.9:g.54401423dup	NCBI36
NG_012133.1:g.4340dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217109.9:c.-33+247dup MANE Select	ENSP00000217109.4:n.-33+247dup
ENST00000217109.8:c.-33+247dup	ENSP00000217109.4:n.-33+247dup
ENST00000415828.5:c.-33+422dup	ENSP00000387968.1:n.-33+422dup
ENST00000428552.1:c.-1+422dup	ENSP00000405171.1:n.-1+422dup
ENST00000452950.1:c.-33+145dup	ENSP00000409035.1:n.-33+145dup
ENST00000490539.1:c.-33+247dup	ENSP00000479273.1:n.-33+247dup
ENST00000493039.5:c.-33+145dup	ENSP00000477958.1:n.-33+145dup
ENST00000498689.5:n.168+422dup
ENST00000613138.1:n.192+247dup
NM_001033521.1:c.-33+422dup	NP_001028693.1:n.-33+422dup
NM_001033522.1:c.-33+145dup	NP_001028694.1:n.-33+145dup
NM_001324.2:c.-33+247dup	NP_001315.1:n.-33+247dup
XM_011528600.1:c.-33+221dup	XP_011526902.1:n.-33+221dup
NM_001033522.2:c.-33+145dup	NP_001028694.1:n.-33+145dup
NM_001324.3:c.-33+247dup MANE Select	NP_001315.1:n.-33+247dup
NM_001033521.2:c.-33+422dup	NP_001028693.1:n.-33+422dup